FdaApplication
ANDA 206468
Identifiers
- fda_app_no: ANDA206468
Properties
| Property | Value |
|---|---|
| applicant_name | NEXUS PHARMACEUTICALS LLC |
| application_type | ANDA |
| approval_date | 2019-02-01 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DICYCLOMINE HYDROCHLORIDE | DICYCLOMINE HYDROCHLORIDE | 10MG/ML | INJECTABLE;INJECTION |
1 product